Canonical Allele Identifier: CA422374082
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1665868602
gnomAD v3: 1-186680784-G-A
gnomAD v4: 1-186680784-G-A
MyVariant Identifiers: chr1:g.186649916G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680784G>A , CM000663.2:g.186680784G>A GRCh38
NC_000001.10:g.186649916G>A , CM000663.1:g.186649916G>A GRCh37
NC_000001.9:g.184916539G>A NCBI36
NG_028206.2:g.4644C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-194C>T (PTGS2) ENSP00000506242.1:n.-194C>T
NR_125801.1:n.131G>A (PACERR)
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